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1
The nature of adrenergic mechanisms involved in anaphylatoxin activity in the guinea-pig.豚鼠过敏毒素活性中肾上腺素能机制的性质。
Br J Pharmacol. 1972 Oct;46(2):260-9. doi: 10.1111/j.1476-5381.1972.tb06871.x.
2
An interaction between exogenously administered anaphylatoxin and histamine in the guinea-pig.外源性施用的过敏毒素与豚鼠体内组胺之间的相互作用。
Arch Int Pharmacodyn Ther. 1972 Oct;199(2):253-65.
3
Modifications of the pressor response to hog renin by adrenalectomy, demedullation, adrenoceptor blocking drugs and catecholamine depletors in anaesthetized rats.肾上腺切除、去髓质、肾上腺素能受体阻断药物及儿茶酚胺耗竭剂对麻醉大鼠对猪肾素升压反应的影响
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4
Definition of the histaminic component of the bronchoconstrictor and cardiovascular effects of anaphylatoxin in the guinea-pig.豚鼠中支气管收缩组胺成分的定义及过敏毒素对心血管的影响。
Br J Pharmacol. 1971 Oct;43(2):424P-425P.
5
Pharmacology of AH 5158; a drug which blocks both - and -adrenoceptors.AH 5158的药理学;一种能阻断α和β肾上腺素能受体的药物。
Br J Pharmacol. 1972 Aug;45(4):660-75. doi: 10.1111/j.1476-5381.1972.tb08125.x.
6
The role of histamine and catecholamines in anaphylatoxin shock as compared to the anaphylactic shock.与过敏性休克相比,组胺和儿茶酚胺在过敏毒素休克中的作用。
Naunyn Schmiedebergs Arch Pharmakol. 1970;266(3):208-22. doi: 10.1007/BF00997283.
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Catecholamines released from the adrenal medulla exert a compensatory, protective effect at beta 2-adrenoceptors against Paf-induced death in mice.从肾上腺髓质释放的儿茶酚胺在β2 -肾上腺素能受体处对血小板活化因子诱导的小鼠死亡发挥代偿性保护作用。
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8
Beta 2- but not beta 1-adrenoceptors mediate the adrenergic component of reflex tracheal dilatation during bronchoconstriction in guinea pigs in vivo.在豚鼠体内支气管收缩期间,β2-而非β1-肾上腺素能受体介导反射性气管扩张的肾上腺素能成分。
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9
Effect of beta-adrenoceptive blocking agents on the response to bronchoconstrictor drugs in the guinea-pig air overflow preparation. Appendix describing a new modification of the air overflow method.β-肾上腺素能阻断剂对豚鼠气道溢流制备中支气管收缩药物反应的影响。描述气道溢流法新改良的附录。
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10
Beta 2-adrenoceptor blockade is the basis of guinea-pig bronchial hyper-responsiveness to leukotriene C4 and other agonists.β2肾上腺素能受体阻滞是豚鼠支气管对白三烯C4和其他激动剂产生高反应性的基础。
Br J Pharmacol. 1983 Aug;79(4):839-48. doi: 10.1111/j.1476-5381.1983.tb10527.x.

引用本文的文献

1
Effects of the C5a anaphylatoxin and its relationship to cyclo-oxygenase metabolites in rabbit vascular strips.C5a过敏毒素对兔血管条的作用及其与环氧化酶代谢产物的关系。
Br J Pharmacol. 1985 Mar;84(3):725-33. doi: 10.1111/j.1476-5381.1985.tb16155.x.
2
Proceedings: A comparison of the histopathological effects of anaphylatoxin (AT) and prostaglandins E2 (PGE2) and F2alpha (PGF2alpha) in guinea-pig lungs.论文集:豚鼠肺中过敏毒素(AT)、前列腺素E2(PGE2)和前列腺素F2α(PGF2α)的组织病理学效应比较
Br J Pharmacol. 1975 Oct;55(2):240P-241P.

本文引用的文献

1
Contributions to the physiology of the lungs: Part I. The bronchial muscles, their innervation, and the action of drugs upon them.对肺生理学的贡献:第一部分。支气管肌肉、其神经支配以及药物对它们的作用。
J Physiol. 1903 Mar 16;29(2):97-173. doi: 10.1113/jphysiol.1903.sp000947.
2
QUANTITATIVE EVALUATION OF GUINEA-PIG ANAPHYLAXIS IN VIVO.豚鼠体内过敏反应的定量评估。
Br J Pharmacol Chemother. 1963 Dec;21(3):441-9. doi: 10.1111/j.1476-5381.1963.tb02012.x.
3
Effect of drugs on the uptake and metabolism of H3-norepinephrine.药物对H3-去甲肾上腺素摄取和代谢的影响。
J Pharmacol Exp Ther. 1961 Nov;134:146-53.
4
Blockade of the actions of adrenaline and noradrenaline.阻断肾上腺素和去甲肾上腺素的作用。
Pharmacol Rev. 1959 Jun;11(2, Part 2):443-61; discussion 462-3.
5
Activation of a histamine-releasing agent (anaphylatoxin) in normal rat plasma.组胺释放剂(过敏毒素)在正常大鼠血浆中的激活。
Br J Exp Pathol. 1954 Oct;35(5):507-18.
6
Evidence for an adrenergic homeostatic bronchodilator reflex mechanism.肾上腺素能稳态支气管扩张反射机制的证据。
Eur J Pharmacol. 1967 Dec;2(3):214-23. doi: 10.1016/0014-2999(67)90090-8.
7
The release and fate of vaso-active hormones in the circulation.血管活性激素在循环中的释放与转归
Br J Pharmacol. 1969 Feb;35(2):209-42. doi: 10.1111/j.1476-5381.1969.tb07982.x.
8
Release of catecholamines in the guinea-pig by substances involved in anaphylaxis.过敏反应相关物质导致豚鼠儿茶酚胺的释放。
Nature. 1967 Feb 25;213(5078):838-40. doi: 10.1038/213838a0.
9
The role of histamine and catecholamines in anaphylatoxin shock as compared to the anaphylactic shock.与过敏性休克相比,组胺和儿茶酚胺在过敏毒素休克中的作用。
Naunyn Schmiedebergs Arch Pharmakol. 1970;266(3):208-22. doi: 10.1007/BF00997283.
10
Actions of anaphylatoxin on circulation and respiration of the guinea pig.
Int Arch Allergy Appl Immunol. 1967;32(5):417-28. doi: 10.1159/000229953.

豚鼠过敏毒素活性中肾上腺素能机制的性质。

The nature of adrenergic mechanisms involved in anaphylatoxin activity in the guinea-pig.

作者信息

Hicks R, Sackeyfio A C

出版信息

Br J Pharmacol. 1972 Oct;46(2):260-9. doi: 10.1111/j.1476-5381.1972.tb06871.x.

DOI:10.1111/j.1476-5381.1972.tb06871.x
PMID:4119694
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1666333/
Abstract
  1. Evidence is presented to elucidate the nature of the adrenergic mechanisms involved in responses of the guinea-pig to anaphylatoxin (AT).2. Investigation by means of adrenalectomy, adrenergic neurone blockade, alpha- and beta- adrenoceptor blockade and exclusion of autonomic reflexes, revealed that the adrenergic mechanisms provoked included catecholamine release from the adrenal medulla, sympathetic reflex activity, stimulation of adrenergic neurones and alpha- and beta-adrenoceptor activity.3. The cardiovascular effects of AT, mediated by histamine release, were largely attributable to adrenal medullary and adrenergic neuronal mechanisms. These mechanisms also exerted a restraint on the predominantly histamine mediated bronchoconstrictor effect of AT.4. The cardiovascular effects of AT activity, not attributable to histamine release, were also probably associated with catecholamine release. However, the bronchoconstrictor component of this AT activity was not significantly affected by guanethidine, and it would, therefore, appear that neuronal bronchodilator mechanisms did not exert a restraint upon this aspect of AT activity.5. These findings are generally compatible with previous work showing that adrenergic mechanisms operate during AT-induced responses. In contrast to previous reports, however, the adrenergic activity was predominantly associated with the effects of released histamine.
摘要
  1. 本文提供了证据以阐明豚鼠对过敏毒素(AT)反应中涉及的肾上腺素能机制的性质。

  2. 通过肾上腺切除术、肾上腺素能神经元阻滞、α和β肾上腺素能受体阻滞以及排除自主反射进行的研究表明,所引发的肾上腺素能机制包括肾上腺髓质释放儿茶酚胺、交感反射活动、肾上腺素能神经元的刺激以及α和β肾上腺素能受体的活动。

  3. 由组胺释放介导的AT的心血管效应在很大程度上归因于肾上腺髓质和肾上腺素能神经元机制。这些机制也对AT主要由组胺介导的支气管收缩效应起到了抑制作用。

  4. AT活性的心血管效应,若不归因于组胺释放,也可能与儿茶酚胺释放有关。然而,这种AT活性的支气管收缩成分不受胍乙啶的显著影响,因此,似乎神经元性支气管扩张机制并未对AT活性的这一方面起到抑制作用。

  5. 这些发现总体上与先前的研究结果一致,即肾上腺素能机制在AT诱导的反应中起作用。然而,与先前的报道不同,肾上腺素能活性主要与释放的组胺的作用相关。